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Estimation of glomerular filtration rate by a radial basis function neural network in patients with type-2 diabetes mellitus
- Xun Liu†1, 2,
- Yan-Ru Chen†1,
- Ning-shan Li†2, 3,
- Cheng Wang1,
- Lin-Sheng Lv4,
- Ming Li1,
- Xiao-Ming Wu2Email author and
- Tan-Qi Lou1Email author
© Liu et al.; licensee BioMed Central Ltd. 2013
Received: 8 October 2012
Accepted: 12 August 2013
Published: 29 August 2013
Accurate and precise estimates of glomerular filtration rate (GFR) are essential for clinical assessments, and many methods of estimation are available. We developed a radial basis function (RBF) network and assessed the performance of this method in the estimation of the GFRs of 207 patients with type-2 diabetes and CKD.
Standard GFR (sGFR) was determined by 99mTc-DTPA renal dynamic imaging and GFR was also estimated by the 6-variable MDRD equation and the 4-variable MDRD equation.
Bland-Altman analysis indicated that estimates from the RBF network were more precise than those from the other two methods for some groups of patients. However, the median difference of RBF network estimates from sGFR was greater than those from the other two estimates, indicating greater bias. For patients with stage I/II CKD, the median absolute difference of the RBF network estimate from sGFR was significantly lower, and the P50 of the RBF network estimate (n = 56, 87.5%) was significantly higher than that of the MDRD-4 estimate (n = 49, 76.6%) (p < 0.0167), indicating that the RBF network estimate provided greater accuracy for these patients.
In patients with type-2 diabetes mellitus, estimation of GFR by our RBF network provided better precision and accuracy for some groups of patients than the estimation by the traditional MDRD equations. However, the RBF network estimates of GFR tended to have greater bias and higher than those indicated by sGFR determined by 99mTc-DTPA renal dynamic imaging.
Diabetic nephropathy is the leading cause of end stage renal disease, a condition characterized by abnormal glomerular filtration rate (GFR) and serum creatinine (SCr) . The National Kidney Foundation (NKF) considers GFR as the best overall measure of kidney function in healthy and diseased individuals . However, measurement of GFR by use of radioisotopes is time-consuming and expensive, so this method is not used in routine clinical practice. Instead, numerous equations have been proposed to estimate the GFR without the need for radioisotopes . These equations consider SCr and several additional variables, such as age, gender, race, and body size . The American Diabetes Association  also recommends estimation of GFR from serum creatinine (SCr) -based formulae, such as a Modification of Diet in Renal Disease (MDRD) study equation .
However, these equations may yield inaccurate estimates in some populations, such as elderly Chinese patients with CKD . Recent studies have criticized the equations currently used to estimate GFR in diabetic patients [6–10]. In particular, the Chronic Kidney Disease Epidemiology Collaboration (CKD-EPI) equation , the Mayo Clinic Quadratic (MCQ) equation , and the four-variable MDRD equation  all underestimated GFR in patients with type-2 diabetes, and the Cockcroft-Gault equation overestimated GFR in patients with type-2 diabetes . These equations may be inaccurate because they do not account for ethnicity . For example, in a group of Chinese patients with CKD, the MDRD equation 7 and the abbreviated MDRD equations underestimated GFR in patients with near-normal renal function and overestimated GFR in patients with advanced renal failure . These equations may also be inaccurate because they were developed by linear regression methods [11, 13, 14]. Linear regression models do not account for the non-linear physiological processes that underlie GFR. Thus, it is important to develop better methodologies for estimation of GFR.
Artificial neural networks (ANNs) have been successfully used to model non-linear phenomena in the field of engineering forecasting. Modern ANNs provide effective nonlinear mapping of data, good fault tolerance, and good self-organization [15, 16]. Previous research demonstrated that an ANN was more accurate than a logistic regression model in prediction of clinical outcome in patients with systemic inflammatory response syndrome and hemodynamic shock . Other research groups have used ANNs to estimate GFR, including a knowledge-based neural network (KBNN) model , an evolving connectionist systems (ECOS) model , and a tree-based model with 6 terminal nodes . In all of these cases, the ANNs provided better estimates of GFR than the traditional equations.
Radial basis function (RBF) networks are among the most widely used ANNs, but there have been limited clinical applications of these networks. Our previous study  described a simple RBF network for estimation of GFR (eGFRRBF) in a group of 327 Chinese patients with chronic kidney disease (CKD). The results indicated that the eGFRRBF had less bias and greater precision than the traditional MDRD equations. The accuracy (deviation less than 30% from the sGFR) of the eGFRRBF was significantly better than those from traditional eGFR equations, such as the Jelliffe-1973-equation and the Ruijin-equation .
In the present study, we tested the precision and accuracy of an RBF network model for estimation of GFR in an independent group of 207 Chinese patients who had type-2 diabetes and CKD and compared the results of the RBF network method with the results from two traditional MDRD formulae .
From January 2005 through December 2009, 207 consecutive patients with type-2 diabetes from the Third Affiliated Hospital of Sun Yat-sen University (Guangzhou, China) were enrolled. Patients younger than 18 years, taking cimetidine or trimethoprim, with acute kidney deterioration, clinical edema, skeletal muscle atrophy, pleural effusion or ascites, malnutrition, amputation, heart failure, or ketoacidosis were excluded. None of the patients were treated by dialysis during the study. CKD was staged according to the National Kidney Foundation (NKF) – Kidney Disease Outcomes Quality Initiative clinical practice guidelines  based on the GFR measured by 99mTc-DTPA dynamic imaging method. Patients were placed into 3 groups based on CKD stage: (i) Stage I/II CKD (GFR ≥ 60 mL/min/1.73 m2); (ii) Stage III CKD (GFR = 30–59 mL/min/1.73 m2); or (iii) Stage IV/V CKD (GFR < 30 mL/min/1.73 m2). The study protocol was approved by the institutional review board at the Third Affiliated Hospital of Sun Yat-sen University and all patients provided informed consent. All participants provided written informed consent.
GFR measured by the 99mTc-DTPA renal dynamic imaging method (modified Gate’s method) was used as the standard GFR (sGFR) [21, 22], and was calculated as described by Li et al. . The gamma camera uptake method with 99mTc-DTPA is a simple method for determination of GFR, and is less time-consuming, and less expensive than other methods . Moreover, this method has been recommended as the reference approach for determination of GFR by the Nephrology Committee of Society of Nuclear Medicine , and is widely used as a standard method for evaluation of kidney function and estimation of GFR in China. 99mTc-DTPA renal dynamic imaging was measured by a Millennium TMMPR SPECT using the General Electric Medical System, as described previously . Serum albumin (Alb) and blood urea nitrogen (BUN) were assayed on a Hitachi 7180 autoanalyzer (Hitachi, Tokyo, Japan; reagents from Roche Diagnostics, Mannheim, Germany). SCr was measured by an enzymatic method on the same instrument according to the manufacturer’s instructions. SRM967 (standard reference material released by NIST for serum creatinine calibration) was used for calibration. Patient sex, age, height, and weight were recorded at the same time.
An ANN is a computational method composed of interconnected artificial neurons (mathematical functions) that processes information and that typically consists of an input layer, one or more hidden layers, and an output layer. ANNs are used in diverse scientific and engineering fields to model the complex relationships of inputs and outputs. An RBF network is a feed-forward network with one hidden layer, in which activation of the hidden layer is a nonlinear radial basis function (a function whose value only depends on the distance to the origin).
In this study, the input layer consisted of measured serum creatinine (SCr) and the output layer consisted of sGFR. Our previous work  indicated that when SCr was measured by the enzymatic method, a simple RBF network model successfully estimated GFR in a population of 327 Chinese patients with CKD, based on analysis of all patients and on analysis of subgroups of patients with different stages of CKD . In this previous study, the RBF network was a feed-forward ANN with an input layer of one unit (SCr), one hidden layer, and an output layer of one unit (sGFR), which was measured in all 327 CKD patients. This RBF network was constructed by use of the newrbe function in MathWorks. In the present study, we tested this RBF network in an independent group of 207 patients who had type-2 diabetes (external validation data set) to verify the original results.
All demographic and clinical data are summarized as means ± standard deviations (SDs), as medians and inter-quartile ranges (IQRs: Q1, Q3) for continuous variables that had non-normal distributions, and as N and percent for categorical data (CKD stage). Data were compared using a one-way ANOVA with Bonferroni’s post hoc correction, the Kruskall Wallis test, the Mann–Whitney U test for pair-wise comparisons of data that had non-normal distributions, or Pearson’s Chi-square test (gender).
The overall differences between eGFR and sGFR are summarized as medians and IQRs due to the non-normal distributions. Differences among patients with different CKD stages were compared with the Kruskall Wallis test with a post hoc method or with the Mann–Whitney U test for pair-wise comparisons. Within-group comparisons of measurements were performed using the Wilcoxon signed ranks test for a given CKD stage.
The accuracy of eGFR are summarized as N and percent of patients with eGFR differing less than 15% (P15), 30% (P30), and 50% (P50) from sGFR. Accuracy of the estimates was compared for patients with different CKD stages using the Pearson Chi-square test. The accuracies of eGFR values were compared using the McNemar test within the same CKD stage. Bland-Altman plots (eGFR4 vs. sGFR, eGFR6 vs. sGFR, and eGFRRBF vs. sGFR) were graphed with Medcalc for Windows (ver. 18.104.22.168, Mariekerke, Belgium). The 3 different methods of estimating GFR were also used to classify patients by CKD stage. A Wilcoxon sign-rank test was used to compare the differences of CKD stages from sGFR and each of these estimates.
All statistical assessments were two-tailed and a p-value less than 0.05 was considered significant. The significance level was adjusted by Bonferroni’s method to 0.0167 (0.05/3) and 0.01 (0.05/4) for post hoc pair-wise comparisons of CKD stages and eGFR, respectively. All statistical analysis was performed using SPSS (version 11.0 SPSS, Chicago IL, USA).
Demographic and clinical characteristics of patients with type-2 diabetes and different stages of CKD (n = 207)
Total1(n = 207)
Stage I/II1(n = 64)
Stage III1(n = 81)
Stage IV/V1(n = 62)
61.43 ± 12.03
56.64 ± 11.65
62.78 ± 11.53a
64.61 ± 11.72a
23.42 (21.45 , 25.83)
23.54 (21.32 , 25.77)
22.86 (21.16 , 25.52)
24.05 (22.04 , 25.92)
1.66 (1.54 , 1.80)
1.66 (1.52 , 1.77)
1.64 (1.54 , 1.81)
1.69 (1.54 , 1.77)
3.75 (3.19 , 4.20)
4.00 (3.51 , 4.41)
3.83 (3.30 , 4.18)
3.39 (2.99 , 3.84)ab
1.52 (0.92 , 3.72)
0.77 (0.57 , 1.09)
1.58 (1.09 , 2.39) a
5.19 (2.99 , 7.01)ab
27.17 (17.76 , 48.54)
16.70 (13.74 , 21.25)
27.90 (18.74 , 44.82)a
54.68 (41.29 , 70.60)ab
DTPA-GFR (mL/min/1.73 m2)
43.45 (25.35 , 64.36)
78.39 (66.86 , 87.89)
43.42 (35.81 , 54.82) a
19.70 (14.58 , 23.19)ab
GFR ≧60 mL/min/1.73 m2
GFR <60 mL/min/1.73 m2
Glomerular filtration rates (sGFR, eGFR 4 , eGFR 6 , and eGFR RBF ) of patients with different stages of CKD
Measurement method (mL/min/1.73 m2)
Total1(n = 207)
Stage I/II1(n = 64)
Stage III1(n = 81)
Stage IV/V1(n = 62)
43.45 (25.35 , 64.36)
78.39 (66.86 , 87.89)
43.42 (35.81 , 54.82)a
19.70 (14.58 , 23.19)ab
42.43 (15.68 , 75.46)
89.12 (67.73 , 124.20)†
42.43 (26.50 , 59.31)a
9.60 (6.71 , 17.11)ab†
39.98 (15.28 , 72.28)‡
90.88 (64.52 , 116.84)‡
40.21 (24.72 , 60.54)a‡
9.92 (6.54 , 17.02)ab†
52.25 (34.21 , 81.64)†‡§
94.23 (70.34 , 115.27)†
50.42 (39.61 , 70.57)a†‡§
24.01 (18.70 , 37.28)ab†‡§
Overall performance of different methods used to estimate glomerular filtration rate in patients with different stages of CKD
Median difference of eGFR and sGFR2
Median absolute difference of eGFR
Total (n = 207)
eGFR4 and sGFR1
-2.83 (-11.23 , 12.13)
32.54 (15.74 , 58.97)
eGFR6 and sGFR1
-4.06 (-12.59 , 11.21)†
32.78 (16.43 , 57.38)
eGFRRBF and sGFR
9.76 (-0.19 , 18.02)†‡
26.24 (13.29 , 55.82)
Stage I/II (n = 64)
eGFR4 and sGFR1
9.23 (-9.20 , 37.35)
26.41 (12.20 , 49.65)
eGFR6 and sGFR1
4.13 (-14.66 , 32.62)†
27.28 (12.73 , 44.42)
eGFRRBF and sGFR
12.03 (-4.98 , 27.83)
19.73 (12.98 , 35.56)†
Stage III (n = 81)
eGFR4 and sGFR1
-1.04 (-12.85 , 9.92)
27.01 (13.76 , 58.47)
eGFR6 and sGFR1
-4.80 (-14.07 , 8.97)†
29.82 (13.65 , 57.57)
eGFRRBF and sGFR
7.96 (-1.22 , 21.47)†‡
25.40 (11.23 , 48.50)
Stage IV/V (n = 62)
eGFR4 and sGFR1
-6.48 (-11.06 , -0.21)
46.90 (30.81 , 64.90)
eGFR6 and sGFR1
-6.99 (-11.23 , -1.63)
46.49 (26.56 , 65.17)
eGFRRBF and sGFR
8.89 (1.95 , 15.48)†‡
49.20 (14.98 , 89.37)
We compared the performance of an RBF neural network in the estimation of GFR with the performance of two traditional GFR estimates based on the MDRD equations (MDRD-4 and MDRD-6) in patients with type-2 diabetes and different stages of CKD. Our results indicate that the RBF network provided more precise estimates of GFR than the MDRD equations, and also provided significantly more accurate estimates of GFR for patients with stage I/II CKD. However, the RBF network also had higher bias than the traditional MDRD equations. In particular, the eGFRRBF tended to over-estimate GFR more than eGFR4 and eGFR6, especially for patients with CKD stage IV/V (Table 2).
In the field of medical data processing, the theoretical basis for the use of statistical regression methods is the “law of large numbers”. That is, the difference of the average of many measurements from the true value should be smaller as more measurements are recorded. However, application of a model derived from one data set to another data set may yield poorer accuracy. Moreover, regression methods can only be used for a limited number of models, and interactions among variables places limits on their use. ANNs have no a priori requirement for data distribution, and can handle multi-collinear input variables, neither of which can be managed by regression methods.
These advantages of ANNs have led to their use in several previous studies for estimation of GFR. Song et al.  used a knowledge-based neural network model (KBNN) for evaluation of renal function based on 441 GFR data vectors from 141 patients. Their proposed GFR prediction model had at least 10% better accuracy than any of the individual regression formulae or a standard neural network model. Marshall et al.  used evolving connectionist systems (ECOS), in which computing structures are trained to generate output from a given set of input variables. They concluded that their ECOS model provided better prediction of GFR in routine clinical practice. No ANNs have been used to estimate GFR of patients with type-2 diabetes mellitus.
It is noteworthy that the RBF network used in this study was only based on SCr measurements, in contrast to the re-expressed MDRD equations, which require measurement of 4 or 6 variables. The NKF does not recommend use of SCr alone for assessment of kidney function . However, previous research indicated that use of fewer variables can yield acceptable estimates of GFR. For example, Bevc et al.  reported that a cystatin C-based estimate, which only requires measurement of serum cystatin C, is a reliable marker of GFR in elderly patients and is comparable to the creatinine-based formulae, including the CKD-EPI formulae. Our results suggest that an RBF model based on a single measurement (SCr) can provide precise and accurate estimates of GFR.
There are several limitations to our study. First, SCr was measured by the enzymatic method. Peake et al.  indicated that the enzymatic creatinine assay, although theoretically more specific, can have interference problems. However, this method produces results for patient samples that agree closely with the results from isotope dilution mass spectrometry (ID-MS). This motivated our use of the re-expressed MDRD equations (MDRD-4 and MDRD-6) instead of the original equation , because the original MDRD equation was developed for use with ID-MS traceable serum creatinine . Second, ANN models can be difficult to display as equations and cannot be readily used without special software, so physicians may be reluctant to accept the results of ANN models. There is need for a platform that can display ANN models and that allows other researchers to readily perform external validation. Third, a previous study-indicated that GFR estimated by 99mTc-DTPA dynamic renal imaging might not better than the modified abbreviated MDRD equation , and the renal dynamic imaging method was less accurate than CKD-EPI equation as well . However, the same study found that the two methods performed similar capability in determining GFR among higher-GFR patients , and 99mTc-DTPA dynamic renal dynamic imaging yields accurate results that are nearly the same as those from measurements of inulin clearance . Rehling et al. showed that a regression line between the values measured by these different methods did not differ from the line of identity . Ma et al. (2007) suggested that, using proper reference GFR, more adequate background subtraction, and soft-tissue attenuation correction may improve the accuracy of 99mTc-DTPA dynamic renal imaging . Finally, our RBF network predicted a higher GFR than that from 99mTc- DTPA renal dynamic imaging. This might be due to differences of participants in the training group (CKD patients with and without diabetes ) and the study group (diabetes patients with and without normal kidney function). Use of more similar training and study groups would provide better external validation and may provide improved results.
A recent survey in China  showed that the prevalence of diabetes was 9.7%, corresponding to 92.4 million people. Although some of the established methods used to estimate GFR are suitable for Chinese patients with CKD , it is important to have more accurate and precise estimations of GFR. In some measures of accuracy and precision, our RBF neural network performed significantly better than the re-expressed MDRD equations in the estimation of GFR. In particular, the IQRs (Table 3) and 95% limits of agreement (Figure 1) for the eGFRRBF were smaller than those from eGFR4 and eGFR6, indicating better precision for the RBF network. However, our data indicated that eGFR estimated by the RBF neural network tended to be higher than the sGFR, and this would result in under-estimation of CKD stage. We suggest that use of an RBF network model with more variables and testing of the model with additional data sets may ultimately provide more accurate and precise estimates of GFR.
In patients with type-2 diabetes, GFR estimated by our RBF network provided better precision and accuracy for some groups of patients than GFR estimated by the traditional MDRD equations. However, the RBF network estimates of GFR tended to have greater bias and higher than those indicated by sGFR determined by 99mTc-DTPA renal dynamic imaging.
We are grateful to the patients for their cooperation.
Sources of support
This work were supported by the National Natural Science Foundation of China (Grant No. 81370866 and 81070612), the China Postdoctoral Science Foundation (Grant No. 201104335), the Guangdong Science and Technology Plan (Grant No. 2011B031800084), the Fundamental Research Funds for the Central Universities (Grant No. 11ykpy38) and the National Project of Scientific and Technical Supporting Programs Funded by Ministry of Science & Technology of China (Grant No. 2011BAI10B05).
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